SODIUM IODIDE- sodium iodide injection, solution

United States - English - NLM (National Library of Medicine)

Buy It Now

Active ingredient:
SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q)
Available from:
Nova-Tech, Inc.
Administration route:
INTRAVENOUS
Prescription type:
PRESCRIPTION
Therapeutic indications:
For use as an aid in the treatment of actinomycosis (lumpy jaw),  actinobacillosis (wooden tongue) and necrotic  stomatitis in cattle. The use of sodium iodide is contraindicated in pregnancy and hyperthyroidism. For Animal Use Only
Authorization status:
unapproved drug other
Authorization number:
65207-819-25

SODIUM IODIDE- sodium iodide injection, solution

Nova-Tech, Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been

approved by FDA. For further information about unapproved drugs, click here.

----------

SODIUM IODIDE 20%

INDICATIONS

For use as an aid in the treatment of actinomycosis (lumpy jaw), actinobacillosis (wooden tongue) and

necrotic stomatitis in cattle.

CONTRAINDICATIONS

The use of sodium iodide is contraindicated in pregnancy and hyperthyroidism.

CAUTION

Animals vary in their susceptibility of iodides. Administer with caution until the animal's tolerance is

determined. Discontinue treatment if adverse reactions occur.

DOSAGE AND ADMINISTRATION:

Using aspetic procedures, administer slowly

by intravenous injection. Inject carefully to

avoid deposition outside of the vein. The usual

dose is 30 mg per pound of body weight (15

mL/100 lb). May be repeated at weekly

intervals, if necessary.

WARNING

Not for use in lactating dairy cows.

For Animal Use Only

Keep Out of Reach Of Children

CAUTION:

Federal law restricts this drug to use

by or on the order of a licensed veterinarian.

COMPOSITION

Each 100 mL of sterile aqueous solution contains:

Sodium Iodide...................20 grams

Water For Injection.................q.s.

Store between 15°C-30°C (59°F-86°F).

TAKE TIME OBSERVE LABEL DIRECTIONS

Manufactured by:

Nova-Tech, Inc.

Grand Island, NE 68801 USA

18-819

RMS 92-366

NDC# 65207-819-25

Net Contents:

250 mL (8.45 fl oz)

Assembled in USA

Lot No.

Exp. Date

SODIUM IODIDE

sodium iodide injection, solution

Product Information

Product T ype

PRESCRIPTION ANIMAL DRUG

Ite m Code (Source )

NDC:6 520 7-8 19

Route of Administration

INTRAVENOUS

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

SO DIUM IO DIDE (UNII: F5WR8 N145C) (IODIDE ION - UNII:0 9 G4I6 V8 6 Q)

IODIDE ION

20 g in 10 0 mL

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

Nova-Tech, Inc.

1

NDC:6 520 7-8 19 -25

250 mL in 1 BOTTLE, PLASTIC

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

unappro ved drug o ther

0 8 /22/20 19

Labeler -

Nova-T ech, Inc. (196078976)

Registrant -

Nova-T ech, Inc. (196078976)

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

No va-Tech, Inc.

19 6 0 78 9 76

manufacture, api manufacture

Revised: 8/2019

Similar products

Search alerts related to this product

View documents history

Share this information